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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

194 related items for PubMed ID: 6345474

  • 21.
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  • 26. Cytogenetic findings in 200 children with mental retardation and multiple congenital anomalies of unknown cause.
    Coco R, Penchaszadeh VB.
    Am J Med Genet; 1982 Jun; 12(2):155-73. PubMed ID: 7102722
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  • 28. Monosomy 8 rescue gave cells with a normal karyotype in a mildly affected man with 46,XY,r(8) mosaicism.
    Gradek GA, Kvistad PH, Houge G.
    Eur J Med Genet; 2006 Jun; 49(4):292-7. PubMed ID: 16829350
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  • 31. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
    Hsu LY.
    Am J Med Genet; 1994 Nov 01; 53(2):108-40. PubMed ID: 7856637
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  • 32. Isochromosome 21 and other chromosomal abnormalities in a patient with erythroleukaemia.
    Werner-Favre C, Cabrol C, Beris P, Engel E.
    Ann Genet; 1983 Nov 01; 26(4):240-2. PubMed ID: 6607706
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  • 33. Brief clinical report: the dup(17p) syndrome.
    Feldman GM, Baumer JG, Sparkes RS.
    Am J Med Genet; 1982 Mar 01; 11(3):299-304. PubMed ID: 7081295
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  • 34. Partial trisomy of chromosome 18 (pter leads to q11): a discussion on the identification of the critical segment.
    San Martin V, Fernandez-Novoa C, Hevia A, Novales A, Fornell J, Galera H.
    Ann Genet; 1981 Mar 01; 24(4):248-50. PubMed ID: 6977308
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  • 36. [Ring chromosome 4 in twins].
    Giuffrè L, Cammarata M, Corsello G, Benigno V, Graziano L, Roccella F, Balsamo V.
    Pediatr Med Chir; 1987 Mar 01; 9(3):349-50. PubMed ID: 3671134
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  • 37. The syndrome of ring chromosome 12.
    Scribanu N, McCullars EB, Baumiller RC, Colon AR.
    Am J Med Genet; 1980 Mar 01; 5(2):165-70. PubMed ID: 7395909
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  • 40. Identification of marker chromosomes in thirteen patients using FISH probing.
    Daniel A, Malafiej P, Preece K, Chia N, Nelson J, Smith M.
    Am J Med Genet; 1994 Oct 15; 53(1):8-18. PubMed ID: 7802042
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